Lymphedema and Paget’s Disease: beyond the nipple

S. Tuzun, Aslinur Keles, Narmin Ahmadli
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Abstract

Lymphedema praecox is a rare lymphatic vascular anomaly diagnosed before the age of 35, presenting with unilateral involvement of the lower extremities. Paget's Disease of Bone (PDB) is also a rare osteometabolic disorder characterized by an accelerated rate of bone remodeling, and diagnosis of the disease is challenging. Here, we report a 49-year-old woman with primary lymphedema since the age of 33, who presented with pain and swelling in her right leg. Although the volume of the extremity diminished after complete decongestive therapy, the pain continued. Further evaluation with X-ray, bone scan, and biochemical markers supported the diagnosis of PDB. Following the zoledronic acid infusion, the pain score improved. However, there is no published association between these two diseases. Both lymphedema and PDB are associated with vascular disease and have a genetic background. This is the first case reporting the coexistence of lymphedema and PDB in the same extremity.
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淋巴水肿与帕吉特氏病:乳头之外
前发性淋巴水肿是一种罕见的淋巴管异常,35 岁以前确诊,表现为单侧下肢受累。帕吉特骨病(Paget's Disease of Bone,PDB)也是一种罕见的骨代谢疾病,其特点是骨重塑速度加快,该病的诊断具有挑战性。在此,我们报告了一名自 33 岁起就患有原发性淋巴水肿的 49 岁女性,她出现右腿疼痛和肿胀。虽然在完全消肿治疗后肢体肿胀有所减轻,但疼痛仍在持续。通过X光、骨扫描和生化指标的进一步评估,她被确诊为原发性淋巴水肿。输注唑来膦酸后,疼痛评分有所改善。然而,这两种疾病之间并没有公开的关联。淋巴水肿和PDB都与血管疾病有关,并有遗传背景。这是首例报告在同一肢体同时存在淋巴水肿和PDB的病例。
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